| ID: 107080644 | CNPY3-GNMT readthrough [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (42929480..42963880) | | |
| ID: 106865373 | GET1-SH3BGR readthrough [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39380326..39515504) | WRB-SH3BGR | |
| ID: 105378828 | CLCA4 antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (86571181..86704493, complement) | | |
| ID: 104909134 | LINC02210-CRHR1 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45620346..45835828) | CRHR1-IT1-CRHR1, MGC57346-CRHR1 | |
| ID: 102723385 | COQ7 divergent transcript [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (19062754..19067691, complement) | | |
| ID: 100885850 | PTGES3L-AARSD1 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42950526..42980528, complement) | | |
| ID: 100652739 | RAET1E antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (149863498..149919508) | RAET1G-AS1 | |
| ID: 100534612 | C1QTNF3-AMACR readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (33986986..34124528, complement) | | |
| ID: 100534611 | TM4SF19-DYNLT2B readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196316085..196338420, complement) | TM4SF19-TCTEX1D2 | |
| ID: 100534595 | HNRNPUL2-BSCL2 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62690262..62727384, complement) | | |
| ID: 100534593 | STX16-NPEPL1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58651253..58715844) | | |
| ID: 100534592 | URGCP-MRPS24 readthrough [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (43866558..43906596, complement) | | |
| ID: 100534589 | HOXA10-HOXA9 readthrough [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (27162438..27180261, complement) | HDSP | |
| ID: 100534012 | TNFAIP8L2-SCNM1 readthrough [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151156649..151170296) | SCNM1 | |
| ID: 100533997 | MAGEA10-MAGEA5 readthrough [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152114049..152138577, complement) | CT1.5, MAGEA10-MAGEA5, MAGEA5P | |
| ID: 100533990 | APOC4-APOC2 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44942238..44949565) | APOC4, Apo-CIV, ApoC-IV | |
| ID: 100533975 | SLMO2-ATP5E readthrough [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (59028678..59042846, complement) | | |
| ID: 100533970 | P2RX5-TAX1BP3 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (3662893..3696404, complement) | P2RX5, P2X5 | |
| ID: 100533955 | SENP3-EIF4A1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7561992..7579006) | | |
| ID: 100533496 | TVP23C-CDRT4 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15436015..15563483, complement) | FAM18B2, FAM18B2-CDRT4, TVP23C | |